Date published: 2025-11-24

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C1orf192 Inhibitors

C1orf192 Inhibitors are a diverse set of chemical compounds that indirectly attenuate the functional activity of C1orf192 through various specific signaling pathways and cellular processes. Staurosporine, LY 294002, Rapamycin, PD 98059, SB 203580, U0126, and SP600125 serve as kinase inhibitors. For instance, Staurosporine broadly inhibits protein kinases potentially affecting C1orf192's phosphorylation status, while LY294002 specifically inhibits PI3K dampening the PI3K/Akt pathway which may be crucial for the stability or localization of C1orf192. Rapamycin, an mTOR inhibitor, and PD 98059, a MEK inhibitor, could interfere with the mTOR and MAPK/ERK pathways, respectively, pathways that might be critical for the functional expression of C1orf192. Similarly, SB 203580, U0126, and SP600125 target the p38 MAPK, MEK1/2, and JNK pathways, respectively, which may also play a role in modulating the activity of C1orf192 if it is indeed regulated by these pathways.

Further along the spectrum of C1orf192 inhibitors are MG-132, Cyclosporin A, 2-Deoxy-D-glucose, Chelerythrine, and W-7. MG-132 inhibits the proteasome, which could lead to the stabilization of proteins that negatively regulate C1orf192, thus reducing its activity. Cyclosporin A, by inhibiting calcineurin, could decrease the activity of NFAT or other calcineurin-dependent factors that may control C1orf192 activity. 2-Deoxy-D-glucose interferes with glycolysis and could affect C1orf192 if it relies on high-energy conditions or is regulated by energy-sensing pathways. Chelerythrine selectively inhibits PKC, which could reduce C1orf192 activity if PKC signaling is involved in its activation or stability. Lastly, W-7 antagonizes calmodulin, which could lead to the inhibition of C1orf192 if calmodulin-dependent signaling is part of its regulatory mechanism. Each of these inhibitors, through their targeted effects on specific cellular signaling pathways and processes, contribute to the collective potential to diminish the functional activity of C1orf192.

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